This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

TIDES USA: Oligonucleotide & Peptide Therapeutics
May 14-17, 2024 | In-Person + Digital
Boston, MA, USAHynes Convention Center

Lubomir Nechev, PhD
Senior Vice President CMC Development at Alnylam Pharmaceuticals, Inc.
Speaker

Profile

Lubomir Nechev, Ph.D. is the Chief CMC Officer of Alnylam Pharmaceuticals. Dr Nechev is oneof the pioneers in the CMC aspects of RNAi therapeutics. He has worked at RibozymePharmaceuticals (RPI), the Nucleic Acids Synthesis unit of Transgenomic, Inc., and has joinedAlnylam in March 2004. In the last 20 years, Dr. Nechev has led the development andimplementation of the CMC strategy for siRNA therapeutics used in five approved products –ONPATTRO®, GIVLAARI®, OXLUMO®, Leqvio®(Novartis), and AMVUTTRA™. The first of them(ONPATTRO®) is also the first approved lipid nanoparticle (LNP) formulated siRNA and thesecond one (GIVLAARI®) is the first approved GalNAc‐conjugated siRNA.Dr. Nechev received his Ph.D. degree in Organic Chemistry from St. Kl. Ohridski University,Sofia, Bulgaria and completed his post‐doctoral training at the Department of Chemistry andCenter in Molecular Toxicology at Vanderbilt University, Nashville, Tennessee.

Agenda Sessions

  • Characterization and Stereochemical Control Strategy of siRNA

    11:10am